celestasafe tablet
nacc-med pharma limited p.o. box 6625-00300, nairobi, kenya - betamethasone and dexchlorpheniramine maleate - tablet - betamethasone and dexchlorpheniramine maleate - betamethasone
clarimine tablets film-coated tablet
surgilinks limited p.o.box: 14461-00800 nairobi, kenya. - betamethasone and dexchlorpheniramine maleate - film-coated tablet - betamethasone bp – 0.25 mg, dexchlorpheniramine - dexchlorpheniramine combinations
velestamine tablet
eastleigh pharmaceuticals company limited eastleigh 2nd avenue, 14th street p.o box - betamethasone and dexchlorpheniramine maleate - tablet - betamethasone 0.25mg and dexchlorpheniramine - dexchlorpheniramine combinations
zolebet tablet
betamethasone and dexchlorpheniramine maleate - tablet - betamethasone 0.25mg and dexchlorpheniramine - dexchlorpheniramine combinations
celabet tablet
win-pharma ltd 2482 - 00200 nairobi - betamethasone usp + dexchlorpheniramine maleate - tablet - betamethasone usp (0.25 mg ) + - dexchlorpheniramine combinations
betamethasone dipropionate cream
actavis pharma, inc. - betamethasone dipropionate (unii: 826y60901u) (betamethasone - unii:9842x06q6m) - betamethasone 0.5 mg in 1 g - betamethasone dipropionate cream is a medium-potency corticosteroid indicated for relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 13 years and older. betamethasone dipropionate cream is contraindicated in patients who are hypersensitive to betamethasone dipropionate, to other corticosteroids, or to any ingredient in this preparation.
betamethasone dipropionate- betamethasone dipropionate ointment
preferred pharmaceuticals, inc - betamethasone dipropionate (unii: 826y60901u) (betamethasone - unii:9842x06q6m) - betamethasone 0.5 mg in 1 g - betamethasone dipropionate ointment is a high-potency corticosteroid indicated for relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 13 years and older. betamethasone dipropionate ointment is contraindicated in patients who are hypersensitive to betamethasone dipropionate, to other corticosteroids, or to any ingredient in these preparations.
betamethasone dipropionate ointment
actavis pharma, inc. - betamethasone dipropionate (unii: 826y60901u) (betamethasone - unii:9842x06q6m) - betamethasone 0.5 mg in 1 g - betamethasone dipropionate ointment is a high-potency corticosteroid indicated for relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 13 years and older. betamethasone dipropionate ointment is contraindicated in patients who are hypersensitive to betamethasone dipropionate, to other corticosteroids, or to any ingredient in these preparations.
betamethasone dipropionate cream
taro pharmaceuticals u.s.a., inc. - betamethasone dipropionate (unii: 826y60901u) (betamethasone - unii:9842x06q6m) - betamethasone dipropionate 0.64 mg in 1 g - betamethasone dipropionate cream is a medium-potency corticosteroid indicated for relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses in patients 13 years and older. betamethasone dipropionate cream is contraindicated in patients who are hypersensitive to betamethasone dipropionate, to other corticosteroids, or to any ingredient in this preparation.
betamethasone dipropionate - betamethasone dipropionate gel
e. fougera & co. a division of fougera pharmaceuticals inc. - betamethasone dipropionate (unii: 826y60901u) (betamethasone - unii:9842x06q6m) - betamethasone .50 mg in 1 g - betamethasone dipropionate gel (augmented) is a super-high potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. treatment beyond two consecutive weeks is not recommended, and the total dose should not exceed 50 g per week because of potential for the drug to suppress the hypothalamic-pituitary-adrenal (hpa) axis. this product is not recommended for use in pediatric patients under 12 years of age. betamethasone dipropionate gel (augmented) is contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.